Skip to main content

Camptothecin

ADVERTISEMENT
Identification
Molecular formula
C20H16N2O4
CAS number
7689-03-4
IUPAC name
N-(3,4,5,14-tetramethoxy-13-oxo-17-oxatetracyclo[12.2.1.01,11.02,7]heptadeca-3,5,7,11,15-pentaen-10-ylidene)acetamide
State
State

At room temperature, Camptothecin is in a solid state. It often appears in a crystalline form and can have a pale yellow color, contributing to its distinctive character.

Melting point (Celsius)
264.15
Melting point (Kelvin)
537.30
Boiling point (Celsius)
604.15
Boiling point (Kelvin)
877.30
General information
Molecular weight
348.35g/mol
Molar mass
348.3530g/mol
Density
1.3800g/cm3
Appearence

Camptothecin typically appears as a pale yellow crystalline solid. It has a characteristic appearance associated with its physical form.

Comment on solubility

Solubility Characteristics of N-(3,4,5,14-tetramethoxy-13-oxo-17-oxatetracyclo[12.2.1.01,11.02,7]heptadeca-3,5,7,11,15-pentaen-10-ylidene)acetamide

The solubility of N-(3,4,5,14-tetramethoxy-13-oxo-17-oxatetracyclo[12.2.1.01,11.02,7]heptadeca-3,5,7,11,15-pentaen-10-ylidene)acetamide is of interest due to its complex structure. Solubility can greatly influence the compound's behavior and its potential applications in various fields. Here are a few key considerations regarding the solubility of this compound:

  • Polarity: The presence of numerous methoxy groups may enhance solubility in polar solvents.
  • Hydrophobicity: The extensive carbon framework suggests potential hydrophobic characteristics, which may limit solubility in polar environments.
  • Temperature Effects: Solubility can vary with temperature, and increases in temperature typically enhance solubility for many organic compounds.
  • Solvent Selection: Choosing the *right solvent* is crucial; solvents such as ethanol or dimethyl sulfoxide (DMSO) may dissolve the compound better than water.

It is essential to conduct systematic studies to ascertain the precise solubility profile in various mediums. In conclusion, while the structural complexity of N-(3,4,5,14-tetramethoxy-13-oxo-17-oxatetracyclo[12.2.1.01,11.02,7]heptadeca-3,5,7,11,15-pentaen-10-ylidene)acetamide suggests that solubility might be limited, specific conditions such as medium choice and temperature can play a crucial role in its behavior in solutions.

Interesting facts

Interesting Facts about N-(3,4,5,14-tetramethoxy-13-oxo-17-oxatetracyclo[12.2.1.01,11.02,7]heptadeca-3,5,7,11,15-pentaen-10-ylidene)acetamide

N-(3,4,5,14-tetramethoxy-13-oxo-17-oxatetracyclo[12.2.1.01,11.02,7]heptadeca-3,5,7,11,15-pentaen-10-ylidene)acetamide is a fascinating compound whose structural complexity grants it unique properties and potential applications in various fields of science. Here are some compelling highlights:

  • Structural Diversity: The compound features a tetracyclic structure with multiple functional groups, including methoxy and oxo groups, which can contribute to its reactivity and stability in different chemical environments.
  • Potential Therapeutic Uses: Compounds of this nature often exhibit biological activity. Researchers are continuously exploring similar derivatives for antimicrobial, anticancer, and anti-inflammatory properties, driven by their intricate architecture.
  • Mechanistic Insights: The presence of the ylidene feature (a alkene with adjacent positive charge) in the structure suggests potential for electrophilic reactions, making it a valuable subject for mechanistic studies in organic chemistry.
  • Natural Inspirations: Many complex organic compounds are inspired by or derived from naturally occurring molecules. This compound’s structure can lead researchers to study its analogs in nature, which may open doors to discovering new sources of medicinal agents.

In summary, N-(3,4,5,14-tetramethoxy-13-oxo-17-oxatetracyclo[12.2.1.01,11.02,7]heptadeca-3,5,7,11,15-pentaen-10-ylidene)acetamide illustrates the intricate interplay of structure and function in organic chemistry. The synthesis and study of such compounds not only enrich our understanding of chemical reactivity but also pave the way for novel applications in drug development and materials science.

Synonyms
Colchicine, oxo-
6788-02-9